Team:The University of Alberta/30 September 2008

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(New page: *Tom can't tell much from the gel2 gel1. <br>)
 
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*Tom
*Tom
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can't tell much from the gel2
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can't tell much from the gel2<br>
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gel1. <br>
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gel1. expected size 3000bp (2-9) and 2000bp(10-16). this is as expected <br>
 +
gel2. expected size 4000bp (1-8) and 4200bp(10-16). result is as expected, but have some short band(contaminations?)<br>
 +
they all seems good! have to sequence to make sure.
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==David==
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starting the bisdA and bisdB cassettes from scratch because i really, really, really want to see if this stuff will work.
 +
 
 +
i digested
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  the correct pTET vector complete with RBS site and 6xHis tag (pTET) with SphI+PstI+CIP treatment
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  BisdA with XbaI+PstI
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  BisdB with XbaI+PstI
 +
 
 +
i gel purified the products and set up the following ligations
 +
 
 +
  pTET+BisdA
 +
  pTET+BisdB

Latest revision as of 03:34, 29 October 2008

  • Tom

can't tell much from the gel2
gel1. expected size 3000bp (2-9) and 2000bp(10-16). this is as expected
gel2. expected size 4000bp (1-8) and 4200bp(10-16). result is as expected, but have some short band(contaminations?)
they all seems good! have to sequence to make sure.


David

starting the bisdA and bisdB cassettes from scratch because i really, really, really want to see if this stuff will work.

i digested

 the correct pTET vector complete with RBS site and 6xHis tag (pTET) with SphI+PstI+CIP treatment
 BisdA with XbaI+PstI
 BisdB with XbaI+PstI

i gel purified the products and set up the following ligations

 pTET+BisdA
 pTET+BisdB